Otolaryngological features in a cohort of patients affected with 22q11.2 deletion syndrome: A monocentric survey-Reference-Cited by-同舟云学术

Otolaryngological features in a cohort of patients affected with 22q11.2 deletion syndrome: A monocentric survey

Published:2018-09-12 Issue:10 Volume:176 Page:2128-2134
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am J Med Genet

Author:

Grasso Fiorentino¹^ORCID,Cirillo Emilia¹,Quaremba Giuseppe²,Graziano Vincenzo²,Gallo Vera¹,Cruoglio Letizia³,Botta Carmine⁴,Pignata Claudio¹^ORCID,Motta Sergio³

Affiliation:

1. Department of Translational Medical Sciences, Pediatric section; Federico II University; Naples Italy

2. Department of Advanced Biomedical Sciences; Federico II University; Naples Italy

3. Department of Neurosciences, Reproductive and Odontostomatological Sciences; Federico II University; Naples Italy

4. Department of Morphologic and Functional Diagnostics, Radiotherapy and Legal Medicine; Federico II University; Naples Italy

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.40518/fullpdf

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3. Otorhinologic Disorders in 22q11.2 Deletion Syndrome;Otolaryngology–Head and Neck Surgery;2023-03-23

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